Product Recalls in Arizona
Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,579 recalls have been distributed to Arizona in the last 12 months.
Showing 28761–28780 of 52,339 recalls
Recalled Item: Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box Recalled by...
The Issue: Several instances of a catheter caught in the sterile barrier seal and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equate Beauty Clarifying Face Daily Moisturizer 4 fl. oz. (118 Recalled by...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Procrit (epoetin alfa) Recalled by Amgen, Inc. Due to Presence of...
The Issue: Presence of particulate matter: glass flakes identified as lamellae observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 14-442000S Antegrade Femoral Nail Instrument Kit Recalled by Zimmer Biomet,...
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument....
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa Recalled by...
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE(R) 100mL EMPTY VINYL CONTAINER With 2 Ports - (5 Boxes of 40)...
The Issue: The hot stamp label on the bag incorrectly states the material of the vinyl...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Aptus Heli-FX Thoracic EndoAnchor System Heli-FX Guide 42 mm...
The Issue: It was determined that the deflection length indicated on the Guide catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT DE handheld data processing module for clinical use Recalled by...
The Issue: Issues resulting from upgrade to software version 2.8: (1) Location,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OTTO BOCK Kenevo knee joints Model 3C60=ST Recalled by Otto Bock Healthcare...
The Issue: Otto Bock Healthcare Products GmbH has identified a design issue through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OTTO BOCK Kenevo knee joints Model 3C60 Recalled by Otto Bock Healthcare...
The Issue: Otto Bock Healthcare Products GmbH has identified a design issue through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeVest Wearable Defibrillator Model 4000 Recalled by Zoll Manufacturing...
The Issue: Incorrect service code for properly catching critical defects during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Implantable Pulse Generator and Infinity 7 Implantable Pulse...
The Issue: Analysis of the difference between the actual device longevity and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim DRG Implantable Pulse Generator Model 3664 Recalled by St. Jude...
The Issue: Analysis of the difference between the actual device longevity and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Medical Kalare Fluoroscopic X-Ray System (DREX-KL80) Kalare is...
The Issue: During an examination images were displayed on the live monitor,but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 5 Elite Implantable Pulse Generator and Proclaim 7 Elite Recalled...
The Issue: Analysis of the difference between the actual device longevity and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BlockAid Cut Resistant Surgical Glove Liners Recalled by Zimmer Biomet, Inc....
The Issue: Cut resistant surgical glove liners lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AndroGel (testosterone gel) 1.62% Recalled by AbbVie Inc. Due to Temperature...
The Issue: Temperature Abuse: Prolonged exposure to temperatures outside of labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AndroGel (testosterone gel) 1.62% Recalled by AbbVie Inc. Due to Temperature...
The Issue: Temperature Abuse: Prolonged exposure to temperatures outside of labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fuji apples Recalled by Apple King, LLC Due to Fuji apples are recalled...
The Issue: Fuji apples are recalled because Thiabendazole was detected at 6.9 ppm.
Recommended Action: Do not consume. Return to store for a refund or discard.